chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116732257	116732258	A	G	35	GENIC	homozygous	116669999
8	116733592	116733594	TG		30	GENIC	heterozygous	133560595
8	116734212	116734213	A	G	48	GENIC	homozygous	116670003
8	116735729	116735730	A	G	7	GENIC	homozygous	116670007
8	116736861	116736862	A	G	47	GENIC	homozygous	116670013
8	116737839	116737840	C	T	59	GENIC	homozygous	117149209
8	116738375	116738375		G	60	GENIC	homozygous	128635208
8	116740312	116740313	A	G	54	GENIC	homozygous	116670025
8	116746767	116746768	C	T	46	GENIC	homozygous	116670059
8	116747054	116747055	C	T	44	GENIC	homozygous	117149211
8	116747437	116747438	A	T	18	GENIC	homozygous	118150733
8	116747711	116747712	C	G	41	GENIC	possibly homozygous	117149212
8	116747885	116747886	G	A	41	GENIC	homozygous	116670063
8	116748143	116748144	C	G	43	GENIC	homozygous	117149213
8	116748664	116748665	G	C	55	GENIC	homozygous	117149214
8	116749214	116749215	A	G	59	GENIC	homozygous	117149215
8	116749399	116749400	A	G	51	GENIC	homozygous	117149216
8	116749414	116749415	C	T	55	GENIC	homozygous	117149217
8	116749994	116749995	A	G	52	GENIC	homozygous	116670071
8	116750338	116750339	A	T	49	GENIC	homozygous	116670073
8	116749962	116749962		TCCCCTC	52	GENIC	homozygous	131054204